Source:http://linkedlifedata.com/resource/pubmed/id/15138266
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
29
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pubmed:dateCreated |
2004-7-12
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pubmed:abstractText |
Tumor necrosis factor-alpha (TNF-alpha) inhibits osteoblast function in vitro by inhibiting collagen deposition. Studies generally support that TNF-alpha does not inhibit collagen biosynthesis by osteoblasts but that collagen deposition is in some way diminished. The study investigated TNF-alpha regulation of biosynthetic enzymes and proteins crucial for posttranslational extracellular collagen maturation in osteoblasts including procollagen C-proteinases, procollagen C-proteinase enhancer, and lysyl oxidase. The working hypothesis is that such regulation could inhibit collagen deposition by osteoblasts. We report that in phenotypically normal MC3T3-E1 osteoblasts, TNF-alpha decreases collagen deposition without decreasing collagen mRNA levels or procollagen protein synthesis. Analyses of the cell layers revealed that TNF-alpha diminished the levels of mature collagen cross-links, pyridinoline and deoxypyridinoline. Further analyses revealed that the mRNA expression for lysyl oxidase, the determining enzyme required for collagen cross-linking, is down-regulated by TNF-alpha in a concentration- and time-dependent manner by up to 50%. The decrease was accompanied by a significant reduction of lysyl oxidase protein levels and enzyme activity. By contrast, Northern and Western blotting studies revealed that procollagen C-proteinases bone morphogenic protein-1 and mammalians Tolloid and procollagen C-proteinase enhancer were expressed in MC3T3-E1 cells and not down-regulated. The data together demonstrate that TNF-alpha does not inhibit collagen synthesis but does inhibit the expression and activity of lysyl oxidase in osteoblasts, thereby contributing to perturbed collagen cross-linking and accumulation. These studies identify a novel mechanism in which proinflammatory cytokine modulation of an extracellular biosynthetic enzyme plays a determining role in the control of collagen accumulation by osteoblasts.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Amino Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Collagen,
http://linkedlifedata.com/resource/pubmed/chemical/Cross-Linking Reagents,
http://linkedlifedata.com/resource/pubmed/chemical/Protein-Lysine 6-Oxidase,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha,
http://linkedlifedata.com/resource/pubmed/chemical/deoxypyridinoline,
http://linkedlifedata.com/resource/pubmed/chemical/pyridinoline
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
16
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pubmed:volume |
279
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
30060-5
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:15138266-Amino Acids,
pubmed-meshheading:15138266-Animals,
pubmed-meshheading:15138266-Blotting, Northern,
pubmed-meshheading:15138266-Blotting, Western,
pubmed-meshheading:15138266-Cell Line,
pubmed-meshheading:15138266-Collagen,
pubmed-meshheading:15138266-Cross-Linking Reagents,
pubmed-meshheading:15138266-Dose-Response Relationship, Drug,
pubmed-meshheading:15138266-Down-Regulation,
pubmed-meshheading:15138266-Inflammation,
pubmed-meshheading:15138266-Mice,
pubmed-meshheading:15138266-Osteoblasts,
pubmed-meshheading:15138266-Protein Structure, Tertiary,
pubmed-meshheading:15138266-Protein-Lysine 6-Oxidase,
pubmed-meshheading:15138266-RNA, Messenger,
pubmed-meshheading:15138266-Time Factors,
pubmed-meshheading:15138266-Tumor Necrosis Factor-alpha
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pubmed:year |
2004
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pubmed:articleTitle |
Regulation of collagen deposition and lysyl oxidase by tumor necrosis factor-alpha in osteoblasts.
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pubmed:affiliation |
Department of Oral Biology, Goldman School of Dental Medicine, Boston University, Boston, Massachussetts 02118, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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